I hope you are all having a wonderful 2022 so far and I would just like to take a moment to thank everyone who has supported us through some of the toughest times and has been there to celebrate the finest.
Set up in 2013 I had no Idea just how much impact Ragdolls UK would have. Over the course of the years our small charity has brought comfort, hope and friendship to hundreds of those affected by Turner’s Syndrome across the UK. We are incredibly proud of this. Like most small charities the current global situation has thrown up even more obstacles but we, like our TS members, may be small but we are mighty. These barriers and obstacles wouldn’t be possible to break if it weren’t for your help.
Turner’s Syndrome is a condition that occurs in 1 in about 2500 female live births across the globe. There are still questions being asked about and still understanding being forged around it. We want to be there for these developments. We too would like to grow and adapt to ever changing information.
With that in mind raising awareness still remains our top priority. Therefore, in February I will be offering a live online discussion on my life with Turner’s Syndrome. I hope to see you all there. Above all, I hope that my story can help my TS sisters embrace their own.
For more information on Turner’s Syndrome, support or projects contact firstname.lastname@example.org